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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345200Generated: October 30, 2026

Chlorine → HCID 15014914, compound

https://huagongshe.com/reaction/345200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorineHCID 24526—
Reactant3-Iodopentafluoroprop-1-eneHCID 2775181—
ReactantSodium HypochloriteHCID 23665760—
CatalystSodium HydroxideHCID 14798—
CatalystTrioctylmethylammonium chlorideHCID 21218—
Catalyst3-Iodopentafluoroprop-1-eneHCID 2775181—
SolventM-XyleneHCID 7929—
ProductHCID 15014914HCID 15014914—

Reaction Conditions

Temperature-10 °C

Reaction Steps

In a 1000-ml flask equipped with a stirring apparatus and a thermometer were charged 100 ml of m-xylene, 500 ml of a sodium hypochlorite aqueous solution having a 12% available chlorine content and containing 5.0 g of sodium hydroxide, 20.0 g (77.5 mmols) of 3-iodopentafluoropropene and 0.25 g (0.6 mmol) of TOMAC as a catalyst. After the reaction liquid was cooled to -10° C., the reaction liquid was stirred with the stirring apparatus to initiate the reaction. The reaction was continued while maitaining the reaction temperature at -10° C. After the 15 minutes of reaction time lapsed, the conversion of 3-iodopentafluoropropene became almost 100%. Then the reaction liquid was cooled to -30° C. to freeze the aqueous phase, and the organic phase was separated therefrom. After the organic phase was dried over anhydrous sodium sulfate, the product was isolated from the organic phase through fractional distillation twice. Thus, 8.7 g (yield, 41%) of the captioned compound having a boiling point of 52° C. was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055601
Source datasetuspto-grants-1991_10
ORD IDord-922e4d5bea7440a79caca8ccc823f242
Source noteuspto-grants-1991_10